HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chroman-4-ol → HCID 15056495, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chroman-4-ol | HCID 92890 | — |
| Reactant | HCID 15056494 | HCID 15056494 | — |
| Reactant | HCID 19888574 | HCID 19888574 | — |
| Reactant | Benzyl 2-oxopropylcarbamate | HCID 22747857 | — |
| Reactant | HCID 67917265 | HCID 67917265 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 15056495 | HCID 15056495 | — |
Reaction Steps
A solution of 1 g of 2-benzyloxycarbonylaminomethyl-2-methyl-4-(1,2-dihydro-2-oxo-1-pyridyl)-6-cyano3-chromene [obtainable from 1-benzyloxycarbonylamino-2-propanone ("1-CBZ-2-propanone") via 2-CBZ-aminomethyl-2-methyl-6-cyano-4-chromanone, the corresponding 4-chromanol, the corresponding 3-chromene and the corresponding 3,4-epoxide] in 20 ml of dioxane is hydrogenated on 0.5 g of 5% Pd-carbon at 20° C. and 1 bar until the calculated amount of H2 has been absorbed. The mixture is filtered, the solution is evaporated and 2-aminomethyl-2-methyl-4-(1,2-dihydro-2-oxo-1-pyridyl)-6-cyano-3-chromene is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05130322 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-171cd426d5c744b0a14a731425883ef1 |
| Source note | uspto-grants-1992_07 |